Synovitis, acne, pustulosis, hyperostosis, osteitis ( <scp>SAPHO</scp> ) syndrome associated with pyoderma gangrenosum: report of two patients-Reference-Cited by-同舟云学术

Synovitis, acne, pustulosis, hyperostosis, osteitis ( SAPHO ) syndrome associated with pyoderma gangrenosum: report of two patients

Published:2022-11-07 Issue:3 Volume:62 Page:
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatology

Author:

Ma Mingwei¹²,Wu Xia³,Cao Yihan⁴,Liu Yuchen¹²,Liu Shengyan¹²,Li Chen²⁵

Affiliation:

1. School of Clinical Medicine Peking Union Medical College Beijing China

2. Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

3. Department of Internal Medicine Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

4. Department of Radiology Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

5. Department of Rheumatology Fangshan Hospital Beijing University of Chinese Medicine Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.16492

Reference5 articles.

1. Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome: review and update

2. A case of neutrophilic dermatoses including pyoderma gangrenosum as a continuous disease spectrum to SAPHO syndrome

3. SAPHO syndrome associated with hidradenitis suppurativa and pyoderma gangrenosum successfully treated with adalimumab and methotrexate: a case report and review of the literature

4. A Case of SAPHO Syndrome with Pyoderma Gangrenosum and Inflammatory Bowel Disease Masquerading as Behçe’s Disease

5. Pyoderma Gangrenosum: An Updated Literature Review on Established and Emerging Pharmacological Treatments

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1. Clinical, epidemiological, and therapeutic hallmarks of pyoderma gangrenosum: a case series of 35 patients;International Journal of Dermatology;2024-02-25